Adverse Event Profile: Ginkgo
Adverse Event Profile: Ginkgo
Source: FDA Center for Food Safety and Applied Nutrition (CFSAN) Adverse Event Reporting System Total Events: 16 Serious Events: 9 Date Range: 20080825 to 20220517
Top Reported Reactions
- DYSPNOEA: 4
- PARAESTHESIA: 2
- SWELLING: 2
- HYPOAESTHESIA: 2
- Haemorrhage: 2
- ANOSMIA: 1
- ASTHENIA: 1
- CONVULSION: 1
- DECREASED APPETITE: 1
- DYSGEUSIA: 1
- LOSS OF LIBIDO: 1
- MEMORY IMPAIRMENT: 1
- SEXUAL DYSFUNCTION: 1
- Coagulopathy: 1
- Epistaxis: 1
- Atrial fibrillation: 1
- Chapped lips: 1
- Chest discomfort: 1
- Dermatitis: 1
- Drug interaction: 1
Outcomes
- Other Serious or Important Medical Event: 11
- Hospitalization: 6
- Other Serious Outcome: 4
- Visited a Health Care Provider: 3
- Disability: 2
- Visited Emergency Room: 2
- Life Threatening: 1
Products Involved (11 unique)
- GINKGO BILOBA
- GINKGO-BILOBA
- GNC HERBAL PLUS STANDARDIZED GINKGO BILOBA HERBAL
- Ginkgo Biloba
- Ginkgo biloba
- NATUREMADE GINKGO BILOBA
- NUTRILITE MEMORY BUILDER WITH GINKGO DIETARY SUPPL
- PURITAN'S PRIDE GINKGO BILOBA
- PURITANS PRIDE GINKGO BILOBA
- WOMEN'S ULTRA MEGA GINKGO BILOBA
- unspecified ginkgo biloba
Disclaimer
This data is from the FDA CAERS database. A report does not mean the supplement caused the adverse event. Reports may be incomplete, duplicated, or unrelated. This is for safety awareness only.